Medicinal agent for suppressing malignant tumor metastasis

ABSTRACT

A medicinal composition for suppressing or preventing the metastasis of a malignant tumor, the composition comprising, as an active ingredient, at least one kind of vasoprotective agent selected from the following (i) to (iv): (i) angiotensin II receptor antagonist, (ii) HMG-CoA reductase inhibitor, (iii) ghrelin or its derivative, and (iv) adrenomedullin or its derivative; or a pharmacologically acceptable salt thereof.

TECHNICAL FIELD

The present invention relates to a novel medicinal composition forsuppressing or preventing the metastasis of a malignant tumor, such ascarcinoma, the agent comprising, as an active ingredient, avasoprotective agent. The present invention also relates to a noveltreatment or prevention method etc. for suppressing or preventing themetastasis of a malignant tumor. The present invention further relatesto a medicinal composition for suppressing or preventing malignant tumorcells from colonizing or invading vascular endothelium, and also relatesto a method for suppressing or preventing malignant tumor cells fromcolonizing or invading vascular endothelium.

BACKGROUND ART

Malignant tumors represented by carcinoma are diseases caused byabnormal growth of cells, and the most distinctive characteristic ofmalignant tumors is invasion into the surrounding tissue and metastasisto other organs. It has been long known that the leading cause of deathfor malignant tumor patients is not the growth of the primary lesion butmultiple organ failure resulting from distant metastasis of the tumorcells. However, control of malignant tumor metastasis has not yet beenachieved so far and is one of the most crucial issues in the whole areaof cancer treatment.

Metastasis of an epithelial malignant tumor (carcinoma) is considered tobe caused by various physiological phenomena of cancer cells, such asthe acquisition of motility and migrating ability typified by epithelialto mesenchymal transition (hereinafter, abbreviated to “EMT”), invasioninto the surrounding tissue, migration and invasion into blood vesselsand lymphatic vessels, colonization in vascular endothelium of distanttissue, metastatic lesion formation, etc.

Also in a non-epithelial malignant tumor (sarcoma etc.), tumor cellsthat have become malignant and acquired motility and migrating abilityinvade blood vessels etc., colonize vascular endothelium of distanttissue, invade the tissue, and then form a metastatic lesion.

In this process, interaction between endothelial selectins of bloodvessels, in particular capillary vessels, and selectin ligands expressedon tumor cells is involved in the colonization of circulating tumorcells in vascular endothelium (Non Patent Literature 1). It is alsoknown that inflammatory cytokines (IL-1β, TNF-α) promote the adhesion oftumor cells to vascular endothelium (Non Patent Literature 2 and 3). Forexample, inflammatory cytokines produced by surgery or a surgery-inducedinfection systemically and locally promote the adhesion of tumor cellsto vascular endothelium and facilitate the metastasis of the tumor cellsto distant tissue and tumor recurrence at the primary site (Non PatentLiterature 1 to 3).

In the prevailing pharmacological treatment for cancer, ananticancer/antitumor agent is administered to a tumor-bearing patientusually for the purpose of reducing the size of the primary focus, andthe effect of the anticancer/antitumor agent is judged by the reductionpercentage. However, an anticancer/antitumor agent is often harmful tonormal tissue, and so-called “adverse effects” that cause various organdisorders appear at a high rate. Therefore, chronic dosing thereofcauses problems of such serious side effects. For this reason, in actualcancer treatment, the administration of anticancer/antitumor agents hasoften to be restricted in terms of the amount and duration, leading toshortened life expectancy.

Ghrelin is a hormone found in the stomach in 1999. For example, theghrelin of a mammal, such as a human, is a peptide having an amino acidsequence composed of 28 residues and having an extremely rare chemicalstructure in which the 3rd amino acid from the N terminus in thesequence is acylated with a fatty acid (Non Patent Literature 4 andPatent Literature 1).

Ghrelin is an endogenous cerebral-gastrointestinal hormone that acts ona growth hormone secretagogue-receptor 1 a (GHS-R1a) and therebypromotes secretion of a growth hormone (GH) from the pituitary (NonPatent Literature 4 and 5).

Recent studies have revealed that ghrelin increases appetite, thatsubcutaneous administration of ghrelin increases body weight and bodyfat, and that ghrelin has activities such as improvement of cardiacfunction (Non Patent Literature 6 to 10). Further, since ghrelin has GHsecretion promoting activity and appetite stimulation activity, it isexpected that ghrelin, through the activity of GH, further effectivelyexerts fat-burning activity for converting fat into energy and theeffect of strengthening muscles through the anabolic activity of GH (NonPatent Literature 11).

Adrenomedullin (hereinafter sometimes referred to as “AM”) is a peptidehaving a strong vasodilating effect. It was first isolated from humanpheochromocytoma, and later immunoreactive AM was detected in varioustissues including lung tissue (Non Patent Literature 12 to 14). AMreceptor expression is abundant in the basal cells of the airwayepithelium and Type II pneumocytes, and the two cell types are involvedin epithelial regeneration of the lung (Non Patent Literature 15). Inrecent studies, it has been shown that AM activates, in vascularendothelial cells, the phosphatidylinositol 3-kinase/Akt dependentpathway, which is considered to regulate many essential steps for cellgrowth (Non Patent Literature 16 to 19).

Angiotensin II has an effect of, via angiotensin II receptors on cellmembrane, constricting blood vessels to raise blood pressure. Therefore,an angiotensin II receptor antagonist can be an effective treatmentagent for circulatory diseases, such as hypertension. A known example ofa preferable chemical structure which exhibits a strong angiotensin IIantagonistic effect is a structure having a biphenyl group substitutedwith a tetrazolyl group, a carboxyl group, or the like on the sidechain. Pharmaceutical compounds having such a structural feature, forexample, losartan, candesartan cilexetil, olmesartan medoxomil, etc. areclinically used as a treatment agent for hypertension (Non PatentLiterature 20, Patent Literature 2 and 3, etc.).

HMG-CoA (3-hydroxy-3-methyl-glutaryl-coenzyme A) reductase inhibitorspecifically inhibits HMG-CoA reductase, which is a rate-limiting enzymeof biosynthesis of cholesterol. It is known that HMG-CoA reductaseinhibitor, which suppresses the synthesis of cholesterol, is effectivein the treatment of hypercholesterolemia, hyperlipoproteinemia,atherosclerosis, etc. (Non Patent Literature 21).

Known examples of the 1st generation of HMG-CoA reductase inhibitorinclude mevinolin, pravastatin, simvastatin, etc., which are a fungalmetabolite or a partially modified product thereof (Patent Literature 4to 6). After the emergence of the 1st generation drugs, syntheticHMG-CoA reductase inhibitors, such as fluvastatin, were developed, whichare known as 2nd generation (Non Patent Literature 22 and PatentLiterature 7).

However, it has been unknown that ghrelin, adrenomedullin, and HMG-CoAreductase inhibitors suppress the metastasis of malignant tumor cells(especially that they suppress the metastasis of a malignant tumorwithout targeting the malignant tumor itself).

Meanwhile, Non Patent Literature 23 describes, regarding angiotensin IIreceptor antagonists, that losartan suppressed the lung metastasis ofrenal cell carcinoma increased by cyclosporin (Cs). Non PatentLiterature 24 describes that losartan suppressed the liver metastasis ofcolon cancer cells. Non Patent Literature 25 describes that candesartansuppressed the lung metastasis of renal cell carcinoma by inhibitingtumor angiogenesis and vascular endothelial growth factor (VEGF)expression. Non Patent Literature 26 describes that candesartansuppressed the lung and liver metastasis of osteosarcoma. Non PatentLiterature 27 describes that candesartan cilexetil (TCV-116) suppressedthe angiogenesis and metastasis of a tumor. Non Patent Literature 28describes that angiotensin II type 1 receptor (AT1 receptor) system isinvolved in the growth, angiogenesis, and metastasis of a tumor.

Also, Non Patent Literature 29 describes that lovastatin as a HMG-CoAreductase inhibitor inhibits E select in expression and inhibits theadhesion of colon cancer cells to human umbilical vein endothelial cells(HUVECs).

Patent Literature 8 discloses medicines for suppressing or preventingthe metastasis of a malignant tumor, the medicines comprising, as anactive ingredient, vascular endothelial intracellular cGMP enhancers,such as natriuretic peptide receptor GC-A agonist, but does not disclosethe effects of ghrelin, adrenomedullin, angiotensin II receptorantagonists, and HMG-CoA reductase inhibitors on the metastasis of amalignant tumor.

CITATION LIST Patent Literature

-   PTL 1: WO 01/07475-   PTL 2: JP-04-364171 A-   PTL 3: JP-05-78328 A-   PTL 4: U.S. Pat. No. 4,231,938-   PTL 5: JP-59-48418 A-   PTL 6: U.S. Pat. No. 4,444,784-   PTL 7: GB Pat. No. 2,202,846-   PTL 8: WO 2012/118042

Non Patent Literature

-   NPL 1: Braedon McDonald et al., Int. J. Cancer 125, 1298-1305 (2009)-   NPL 2: Miranda Ten Kate et al., Int. J. Cancer 112, 943-950 (2004)-   NPL 3: Ge Yu at al., Surg Endosc, 24, 2860-2870 (2010)-   NPL 4: Kojima at al., Nature, 402, 656-660 (1999)-   NPL 5: Howard at al., Science, 273, 974-977 (1996)-   NPL 6: Wren at al., Endocrinology, 141, 4325-4328 (2000)-   NPL 7: Nakazato at al., Nature, 409, 194-198 (2001)-   NPL 8: Shintani at al., Diabetes, 50, 227-232 (2001)-   NPL 9: Lely at al., Endocr. Rev., 25, 656-660 (2004)-   NPL 10: Korbonits at al., Front Neuroendocrinol., 25, 27-68 (2004)-   NPL 11: Kangawa at al., J. Pharmacol. Sci., 100, 398-410 (2006)-   NPL 12: Kitamura K at al., Biochem Biophys Res Commun, 192, 553-560    (1993)-   NPL 13: Ichiki Y at al., FEBS Lett, 338, 6-10 (1994)-   NPL 14: Sakata J at al., FEBS Lett, 352, 105-108 (1994)-   NPL 15: Martinez A at al., J Histochem Cytochem, 45, 159-164 (1997)-   NPL 16: Nishimatsu H at al., Circ Res, 89(1), 63-70 (2001)-   NPL 17: Shiojima I at al., 90, 1243-1250 (2002)-   NPL 18: Kim W at al., FASEB J, 17, 1937-1939 (2003)-   NPL 19: Tokunaga N at al., Circulation, 109, 526-531 (2004)-   NPL 20: Ruth R. Wexler at al., Journal of Medicinal Chemistry, 39,    625 (1996)-   NPL 21: Am. J. Med., 104(2A), 193 (1998)-   NPL 22: F. G. Kathawala et al, 8th Int'l Symp. on Atherosclerosis,    Abstract Papers, 445, Rome (1988)-   NPL 23: M. Maluccio at al., Transplantation Proceedings, 33,    1820-1821 (2001)-   NPL 24: Luo at al., Pathobiology, 78, 285-290 (2011)-   NPL 25: Maejima et al., Cancer Research, 62, 4176-4179 (2002)-   NPL 26: Wasa et al., Anticancer Research, 31, 123-128 (2011)-   NPL 27: Fujita et al., Biochemical and Biophysical Research    Communication, 294, 441-447 (2002)-   NPL 28: Ino at al., Expert Opinion on Biological Therapy, 6(3),    243-255 (2006)-   NPL 29: Tobias Nubel at al., FASEB J., 18(1), 140-2 (2004)

SUMMARY OF INVENTION Technical Problem

A major objective of the present invention is to provide a novelmedicinal composition etc. for suppressing or preventing the metastasisof a malignant tumor, such as carcinoma. Another objective of thepresent invention is to provide a novel treatment or prevention methodfor suppressing or preventing the metastasis of a malignant tumor.Another objective of the present invention is to provide a medicinalcomposition for suppressing or preventing malignant tumor cells fromcolonizing or invading vascular endothelium, and also a method forsuppressing or preventing malignant tumor cells from colonizing orinvading vascular endothelium. Other objectives of the present inventionwill become clear from the following descriptions.

Solution to Problem

The present inventors made extensive examination to solve the problemsdescribed above. As a result, they found that treatment with use of ananticancer/antitumor agent can exacerbate or augment the distantmetastasis of a cancer and that vasoprotective agents including anangiotensin II receptor antagonist, a HMG-CoA reductase inhibitor,ghrelin, and adrenomedullin can effectively suppress the exacerbation oraugmentation of cancer metastasis. Based on the findings, they completedthe present invention.

An angiotensin II receptor antagonist, a HMG-CoA reductase inhibitor,ghrelin, and adrenomedullin, as vasoprotective agents, can actprotectively on vascular endothelium and thereby effectively inhibit thecolonization (adhesion) and invasion of malignant tumor cells tovascular endothelium during the process of metastasis. The adhesion andinvasion of malignant tumor cells to vascular endothelium are processescommon to metastasis of tumor cells. Therefore, by inhibiting malignanttumor cells from colonizing or invading vascular endothelium, themetastasis of any and all malignant tumors can be suppressed orprevented effectively. Such a metastasis suppressing effect based on avasoprotective effect is different from the effect that is exerted on amalignant tumor itself and suppresses the growth and metastasis of thetumor by inhibiting angiogenesis or by suppressing DNA synthesis in amalignant tumor.

In the present invention, the metastasis of a malignant tumor (cells)includes distant metastasis of a malignant tumor (cells) and recurrenceof a malignant tumor (recurrence at the site of the primary lesion(primary tumor)). The “suppressing or preventing the metastasis of amalignant tumor” means suppressing or preventing distant metastasis of amalignant tumor and/or suppressing or preventing recurrence of amalignant tumor (recurrence at the site of the primary lesion).

That is, the present invention relates to the following.

(1) A medicinal composition for suppressing or preventing the malignanttumor metastasis, the composition comprising, as an active ingredient,at least one kind of vasoprotective agent selected from the following(i) to (iv):

(i) angiotensin II receptor antagonist,(ii) HMG-CoA reductase inhibitor,(iii) ghrelin or its derivative, and(iv) adrenomedullin or its derivative;or a pharmacologically acceptable salt thereof.

(2) A medicinal composition for suppressing or preventing exacerbationand/or augmentation of metastasis of a malignant tumor caused by ananticancer and/or antitumor agent, the composition comprising, as anactive ingredient, at least one kind of vasoprotective agent selectedfrom the following (i) to (iv):

(i) angiotensin II receptor antagonist,(ii) HMG-CoA reductase inhibitor,(iii) ghrelin or its derivative, and(iv) adrenomedullin or its derivative;or a pharmacologically acceptable salt thereof.

The present invention also relates to a treatment or prevention methodfor suppressing or preventing the metastasis of a malignant tumor, themethod comprising administering, to a patient, an effective amount of atleast one kind of vasoprotective agent selected from the above (i) to(iv) and a pharmacologically acceptable salt thereof.

The present invention also relates to a treatment or prevention methodfor suppressing or preventing exacerbation and/or augmentation ofmetastasis of a malignant tumor caused by an anticancer and/or antitumoragent, the method comprising administering, to a patient, an effectiveamount of at least one kind of vasoprotective agent selected from theabove (i) to (iv) or a pharmacologically acceptable salt thereof.

The present invention also relates to at least one kind ofvasoprotective agent selected from the above (i) to (iv) or apharmacologically acceptable salt thereof for use in suppressing orpreventing the metastasis of a malignant tumor.

The present invention also relates to at least one kind ofvasoprotective agent selected from the above (i) to (iv) or apharmacologically acceptable salt thereof for use in suppressing orpreventing exacerbation and/or augmentation of metastasis of a malignanttumor caused by an anticancer and/or antitumor agent.

The present invention also encompasses a medicinal composition forsuppressing or preventing the colonization or invasion of malignanttumor cells to vascular endothelium, the composition comprising, as anactive ingredient, at least one kind of vasoprotective agent selectedfrom the above (i) to (iv) or a pharmacologically acceptable saltthereof.

The present invention also encompasses a method for suppressing orpreventing the colonization or invasion of malignant tumor cells tovascular endothelium, the method comprising administering, to a patient,an effective amount of at least one kind of vasoprotective agentselected from the above (i) to (iv) and a pharmacologically acceptablesalt thereof.

The present invention also encompasses at least one kind ofvasoprotective agent selected from the above (i) to (iv) or apharmacologically acceptable salt thereof for use in suppressing orpreventing the colonization or invasion of malignant tumor cells tovascular endothelium.

Many of treatment agents against malignant tumor metastasis that arecurrently used or under development suppress the metastasis through amechanism of controlling malignant tumor itself. However, the targettissue of the present invention is blood vessels and perivascular tissue(preferably vascular endothelium but not limited to vascular endothelialcells), and the malignant tumor metastasis suppressing effect is exertedby controlling the host side. The treatment method has a completelydifferent mechanism from the conventional one and is a novel technologyapplicable to any and all malignant tumors regardless of the kind or thenature of the malignant tumor. For example, the present invention cansuppress or prevent the colonization or invasion of malignant tumorcells to vascular endothelium, and owing to such a vasoprotectiveeffect, can effectively suppress or prevent the metastasis of amalignant tumor.

Advantageous Effects of Invention

The medicinal composition, the treatment or prevention method, etc. ofthe present invention have an excellent effect of effectivelysuppressing or preventing the metastasis of a malignant tumor. Inparticular, the medicinal composition, the treatment or preventionmethod, etc. of the present invention can effectively suppress orprevent the metastasis of a malignant tumor through a vasoprotectiveeffect. For example, the medicinal composition and the treatment orprevention method of the present invention can suppress or prevent thecolonization or invasion of malignant tumor cells to vascularendothelium in the process of the metastasis of a malignant tumor. Thus,the medicinal composition and the treatment or prevention method of thepresent invention can exert an excellent metastasis suppressing orpreventing effect.

The inventors of the present invention found that administration of ananticancer/antitumor agent (for example, a platinum-based antitumoragent, such as cisplatin (CDDP)) causes vascular endothelial disorder,which promotes the adhesion and invasion of a malignant tumor tovascular endothelium and thus facilitates the metastasis of a malignanttumor. The medicinal composition of the present invention, through itsvasoprotective effect, suppresses the adhesion of a malignant tumor tovascular endothelium promoted by administration of ananticancer/antitumor agent, and thus exerts an excellent tumormetastasis suppressing effect (tumor metastasis (distant tumormetastasis) suppressing effect and/or tumor recurrence suppressingeffect). Therefore, the use of the medicinal composition of the presentinvention effectively suppresses or prevents exacerbation and/oraugmentation of metastasis of a malignant tumor caused by an anticancerand/or antitumor agent.

Further, the medicinal composition of the present invention, through itsvasoprotective effect, can suppress systemic and local adhesion ofmalignant tumor cells to vascular endothelial cells promoted by surgery,and thus has an excellent tumor metastasis suppressing effect.

With such excellent effects, the present invention can prevent orsuppress the metastasis of a malignant tumor, prevent the recurrenceafter therapeutic resection of a tumor, and also effectively suppress orprevent the metastasis of a malignant tumor that is hard to resect. As aresult, an extended survival period can be obtained.

Angiotensin II receptor antagonists, such as telmisartan; HMG-CoAreductase inhibitors, such as pitavastatin; etc. have already beenclinically administered to a large number of patients, and the safetyhas been confirmed. In addition, ghrelin and adrenomedullin are peptidespresent in the body of mammals including humans. Therefore, themedicinal composition, the treatment or prevention method, etc. of thepresent invention have little risk of adverse effects and have anexcellent tumor metastasis suppressing effect. Thus, the medicinalcomposition, the treatment or prevention method, etc. of the presentinvention have both a high safety and an excellent tumor metastasissuppressing effect, and thus are useful in the prevention, treatment,recurrence prevention, etc. of a malignant tumor.

BRIEF DESCRIPTION OF DRAWINGS

FIG. 1 shows micrographs of lungs at 2 weeks from the injection of mousemelanoma B16-F10 tumor cells into the tail vein of mice in a tail veininjection metastasis test where CDDP, ghrelin, and adrenomedullin wereadministered (A: the lungs of a mouse as a control, B: the lungs of amouse to which CDDP was administered, C: the lungs of a mouse to whichadrenomedullin was administered, D: the lungs of a mouse to whichghrelin was administered). Black parts are nodules (metastatic foci)formed by metastasized melanoma.

FIG. 2 shows a graph showing the number of nodules formed due to lungmetastasis at 2 weeks from the injection of mouse melanoma B16-F10 tumorcells into the tail vein of mice in a tail vein injection metastasistest where CDDP, ghrelin, and adrenomedullin were administered. Thevertical axis indicates the number of nodules formed in the lungs perindividual. Each bar is for, from the left to the right, the controlgroup (physiological saline), the CDDP group (5 mg/kg), theadrenomedullin group (0.05 μg/kg/min), and the ghrelin group (0.08μg/kg/min).

FIG. 3 shows micrographs of lungs at 14 days from the injection of mousemelanoma B16-F10 tumor cells into the tail vein of mice in a tail veininjection metastasis test where telmisartan (2 mg/kg or 8 mg/kg) andangiotensin II (1 μg/kg/min) were administered alone, or telmisartan (2mg/kg or 8 mg/kg) was administered before pretreatment with CDDP (5mg/kg). Black parts are nodules (metastatic foci) formed by metastasizedmelanoma.

FIG. 4 shows a graph showing the number of nodules formed due to lungmetastasis at 14 days from the injection of mouse melanoma B16-F10 tumorcells into the tail vein of mice in a tail vein injection metastasistest where telmisartan (2 mg/kg or 8 mg/kg) was administered alone, ortelmisartan (2 mg/kg or 8 mg/kg) was administered before pretreatmentwith CDDP (5 mg/kg). The vertical axis indicates the number of nodulesformed in the lungs per individual. Each bar is for, from the left tothe right, the control group (physiological saline), the telmisartan 2mg/kg group, the telmisartan 8 mg/kg group, the CDDP group (5 mg/kg),the group to which telmisartan 2 mg/kg was administered before CDDPpretreatment, and the group to which telmisartan 8 mg/kg wasadministered before CDDP pretreatment.

FIG. 5 shows micrographs of lungs at 14 days from the injection of mousemelanoma B16-F10 tumor cells into the tail vein of mice in a tail veininjection metastasis test where pitavastatin (20 mg/kg) was administeredalone, or pitavastatin (20 mg/kg) was administered before pretreatmentwith CDDP (5 mg/kg). Black parts are nodules (metastatic foci) formed bymetastasized melanoma.

FIG. 6 shows a graph showing the number of nodules formed due to lungmetastasis at 14 days from the injection of mouse melanoma B16-F10 tumorcells into the tail vein of mice in a tail vein injection metastasistest where pitavastatin (20 mg/kg) was administered alone, orpitavastatin (20 mg/kg) was administered before pretreatment with CDDP(5 mg/kg). The vertical axis indicates the number of nodules formed inthe lungs per individual. Each bar is for, from the left to the right,the control group (physiological saline), the CDDP group (5 mg/kg), thepitavastatin group (20 mg/kg), and the group to which pitavastatin (20mg/kg) was administered before CDDP pretreatment.

FIG. 7 shows micrographs of lungs at 14 days from the injection of mousemelanoma B16-F10 tumor cells into the tail vein of mice in a tail veininjection metastasis test where CDDP (5 mg/kg) was administered alone,or CDDP (5 mg/kg) was administered with valsartan, losartan, olmesartanmedoxomil, azilsartan, candesartan cilexetil, or irbesartan (A: thelungs of a mouse as a control, B: the lungs of a mouse to which CDDP (5mg/kg) was administered, C: the lungs of a mouse to which CDDP (5 mg/kg)and valsartan (40 mg/kg) were administered, D: the lungs of a mouse towhich CDDP (5 mg/kg) and losartan (30 mg/kg) were administered, E: thelungs of a mouse to which CDDP (5 mg/kg) and olmesartan medoxomil (5mg/kg) were administered, F: the lungs of a mouse to which CDDP (5mg/kg) and azilsartan (10 mg/kg) were administered, G: the lungs of amouse to which CDDP (5 mg/kg) and candesartan cilexetil (8 mg/kg) wereadministered, H: the lungs of a mouse to which CDDP (5 mg/kg) andirbesartan (100 mg/kg) were administered). Blackparts are nodules(metastatic foci) formed by metastasized melanoma.

FIG. 8 shows a graph showing the number of nodules formed due to lungmetastasis at 14 days from the injection of mouse melanoma B16-F10 tumorcells into the tail vein of mice in a tail vein injection metastasistest where CDDP (5 mg/kg) was administered alone, or CDDP (5 mg/kg) wasadministered with valsartan, losartan, olmesartan medoxomil, azilsartan,candesartan cilexetil, or irbesartan. The vertical axis indicates thenumber of nodules formed in the lungs per individual. Each bar is for,from the left to the right, the control group (physiological saline),the CDDP group (5 mg/kg), the group to which CDDP (5 mg/kg) andvalsartan (40 mg/kg) were administered, the group to which CDDP (5mg/kg) and losartan (30 mg/kg) were administered, the group to whichCDDP (5 mg/kg) and olmesartan medoxomil (5 mg/kg) were administered, thegroup to which CDDP (5 mg/kg) and azilsartan (10 mg/kg) wereadministered, the group to which CDDP (5 mg/kg) and candesartancilexetil (8 mg/kg) were administered, and the group to which CDDP (5mg/kg) and irbesartan (100 mg/kg) were administered.

FIG. 9 shows the results of co-culture carried out as follows. Humanlung arterial microvascular endothelial cells were cultured toconfluence, losartan was added thereto (to a final concentration of5×10⁻⁶ M), and 2 hours later, phosphate buffered saline (PBS) orcisplatin (CDDP) was added (to a final concentration of 5 μM). An hourlater, the culture medium was replaced with a fresh culture medium(Medium 199 containing 1% BSA). To this, a suspension offluorescently-labeled A549 human lung cancer cells (1×10⁵ cells) wasadded, and the cells were co-cultured for 3 hours. After the co-culture,non-adherent cancer cells were washed out with cold PBS, and then15-minute fixation with 4% formalin was performed. FIG. 9A showsphotographs (fluorescence micrograph) of fluorescently-labeled A549cells, and FIG. 9B shows a graph of the number of adherent cancer cellsin a field of view (×4.2) obtained with an automated cell counter. InFIG. 9A, spots which appear gray (actually green) arefluorescently-labeled A549-GFP human lung cancer cells. In FIG. 9B,white bars are for the control (without losartan pretreatment), andblack bars are for the cases with losartan pretreatment. The verticalaxis indicates the number of cancer cells that adhered (*: P<0.05).

DESCRIPTION OF EMBODIMENTS

Examples of the vasoprotective agent of the present invention includeghrelin or its derivative, adrenomedullin or its derivative, anangiotensin II receptor antagonist, and a HMG-CoA reductase inhibitor.Among them, preferred are ghrelin or its derivative, adrenomedullin orits derivative, and an angiotensin II receptor antagonist, andparticularly preferred is an angiotensin II receptor antagonist.

Ghrelin and its Derivatives:

Ghrelin acts on a growth hormone secretagogue-receptor 1 a (GHS-R1a) andthereby promotes secretion of a growth hormone (GH) from the pituitary.

Also, ghrelin has an amino acid sequence usually composed of 28 aminoacid residues (or 27 amino acid residues) and having a structure inwhich the 3rd amino acid residue from the N terminus is acylated with afatty acid.

In more detail, regarding human or nonhuman mammalian (rat, mouse,porcine, bovine, equine, ovine, canine, etc., for example) ghrelin, thefollowing amino acid sequences and acylated structure are known(aforementioned Patent Literature 1).

Human: (SEQ ID NO: 1) GSS(n-octanoyl)FLSPEHQRVQQRKESKKPPAKLQPR(SEQ ID NO: 2) GSS(n-octanoyl)FLSPEHQRVQRKESKKPPAKLQPR Rat:(SEQ ID NO: 3) GSS(n-octanoyl)FLSPEHQKAQQRKESKKPPAKLQPR (SEQ ID NO: 4)GSS(n-octanoyl)FLSPEHQKAQRKESKKPPAKLQPR Mouse: (SEQ ID NO: 5)GSS(n-octanoyl)FLSPEHQKAQQRKESKKPPAKLQPR Porcine: (SEQ ID NO: 6)GSS(n-octanoyl)FLSPEHQKVQQRKESKKPAAKLKPR Bovine: (SEQ ID NO: 7)GSS(n-octanoyl)FLSPEHQKLQRKEAKKPSGRLKPR Ovine: (SEQ ID NO: 8)GSS(n-octanoyl)FLSPEHQKLQRKEPKKPSGRLKPR Canine: (SEQ ID NO: 9)GSS(n-octanoyl)FLSPEHQKLQQRKESKKPPAKLQPR Equine: (SEQ ID NO: 10)GSS(n-butanoyl)FLSPEHHKVQHRKESKKPPAKLKPR(In the above expression, each amino acid residue is represented by thesingle character expression).

As shown above, ghrelin has a structure in which the side chain hydroxylgroup of the amino acid residue (serine (S) residue etc.) at the 3rdposition from the N terminus is acylated with a fatty acid, such asoctanoic acid and decanoic acid.

For example, human ghrelin is a peptide having an amino acid sequencerepresented by SEQ ID NO: 1 or 2 in which the amino acid residue (serineresidue) at the 3rd position from the amino terminus is a modified aminoacid residue having a side chain (hydroxyl group) acylated with a fattyacid (n-octanoic acid).

As the ghrelin, preferred is mammalian ghrelin. For example, human ornonhuman mammalian (rat, mouse, porcine, bovine, equine, ovine, canine,etc.) ghrelin can be used. It is preferred for each individual to useghrelin of the same species. For example, it is preferred for a human touse human ghrelin.

Examples of the ghrelin derivative include those having a structuresimilar to that of ghrelin and having effects similar to those ofghrelin, i.e., an agonistic effect on a growth hormonesecretagogue-receptor 1 a (GHS-R1a) and an effect of promoting secretionof a growth hormone (GH) from the pituitary.

Specific examples of the ghrelin and its derivative include a peptidehaving a structure selected from the following (1) to (3) and having anagonistic effect on growth hormone secretagogue receptor 1 a.

(1) A peptide having an amino acid sequence represented by any one ofSEQ ID NOs: 1 to 10 in which the amino acid residue at the 3rd positionfrom the amino terminus is a modified amino acid residue having a sidechain acylated with a fatty acid;

(2) A peptide having an amino acid sequence represented by any one ofSEQ ID NOs: 1 to 10 in which one to several amino acids are deleted,substituted, and/or added and the amino acid residue at the 3rd positionfrom the amino terminus is a modified amino acid residue having a sidechain acylated with a fatty acid;

(3) A peptide having an amino acid sequence represented by any one ofSEQ ID NOs: 1 to 10 in which the sequence from the amino terminus to atleast the 4th position is conserved, one to several amino acids aredeleted, substituted, and/or added not in the conserved sequence, andthe amino acid residue at the 3rd position from the amino terminus is amodified amino acid residue having a side chain acylated with a fattyacid.

The “amino acid sequence represented by any one of SEQ ID NOs: 1 to 10”in the above (1) to (3) is, for example in cases where the medicinalcomposition of the present invention is applied to a human, preferably“an amino acid sequence represented by SEQ ID NO: 1 or 2”.

Examples of the fatty acid introduced into the side chain in the above(1) to (3) include fatty acids having 2, 4, 6, 8, 10, 12, 14, 16, or 18carbon atoms, preferably octanoic acid, decanoic acid, or a monoenoic orpolyenoic acid thereof, and more preferably octanoic acid (having 8carbon atoms, n-octanoic acid, etc.).

In the above (2) and (3), the number of amino acids intended in the “oneto several amino acids are deleted, substituted, and/or added”(hereinafter the “deleted, substituted, and/or added” is sometimesreferred to as “substituted or the like”) is not particularly limited aslong as the peptide consisting of the amino acid sequence or itsderivative has the desired effect (i.e., an agonistic effect on growthhormone secretagogue receptor 1 a). The number is, for example, about 1to 9, preferably about 1 to 4, more preferably about 1 to 3, still morepreferably about 1 to 2, and particularly preferably about 1. As usedherein, addition includes insertion. In cases of substitution or thelike with amino acids having similar properties (charge and/orpolarity), the desired functions are generally retained even if not afew amino acids have been substituted or the like. In cases wheresubstitution or the like occurs at two or more positions, thesubstitution or the like in all the positions may be deletion only,substitution only, or addition only, or a combination of two or more ofdeletion, substitution, and addition.

In the amino acid sequence of the ghrelin derivative (for example, theabove (2) and (3)), it is preferred that the sequence from the aminoterminus to at least the 4th position, preferably to the 5th position,more preferably to the 10th position of the amino acid sequence ofnatural ghrelin (for example, an amino acid sequence represented by anyone of SEQ ID NOs: 1 to 10) is conserved.

Preferably, the amino acid sequence of the ghrelin derivative (forexample, the above (2) and (3)) usually has sequence homology of about70% or more, preferably about 80% or more, more preferably about 90% ormore, particularly preferably about 95% or more, and most preferablyabout 97% or more as compared with the amino acid sequence of naturalghrelin.

Examples of other ghrelin derivatives include those in which thecarboxyl terminus of the above-exemplified structure is not ended as acarboxylic acid but amidated so as to mimic a peptide bond. Such a formmakes it possible to find out the minimum unit of activity in a shorteramino acid sequence. Another example of other ghrelin derivatives may bethe one in which a basic amino acid is added or an amino acid in theform of an amide, such as -Lys-NH₂, is introduced to the carboxylterminus as desired.

Other ghrelin derivatives can be designed appropriately referring to,for example, literature by Matsumoto et al. (Structural similarity ofghrelin derivatives to peptidyl growth hormone secretagogues. Matsumoto,M, Kitajima Y, Iwanami T, Hayashi Y, Tanaka S, Minamitake Y, Hosoda H,Kojima M, Matsuo H, Kangawa K. Biochem Biophys Res Commun. 2001 Jun. 15;284(3): 655-9).

Whether the ghrelin or its derivative has an agonistic effect on growthhormone secretagogue receptor 1 a can be determined by the methoddescribed in literature by Matsumoto et al. (Structure-activityrelationship of ghrelin: pharmacological study of ghrelin peptides.Matsumoto M, Hosoda H, Kitajima Y, Morozumi N, Minamitake Y, Tanaka, S,Matsuo H, Kojima M, Hayashi Y, and Kangawa K. Biochem Biophys ResCommun. 2001 Sep. 14; 287(1): 142-6.) using, as an indicator,physiological effect via growth hormone secretagogue receptor 1 a, suchas increase in intracellular calcium ion concentration.

In more detail, for example, ghrelin or its derivative is brought intocontact with growth hormone secretagogue receptor 1 a, and whether theghrelin or its derivative increases intracellular calcium ionconcentration by binding to the receptor is examined. When the increasein intracellular calcium ion concentration is observed, the compound isregarded as having the agonistic effect.

Examples of other forms of the ghrelin derivative include a nucleic acidwhich encodes ghrelin or a ghrelin derivative having a peptide structureas described above. The nucleic acid should be designed to express, whenadministered in vivo, ghrelin or its derivative having the peptidestructure as described above.

Ghrelin and its derivative can be synthesized by a conventional method,for example, a chemical synthesis. For example, amino acids withprotecting groups are condensed by a liquid phase method and/or a solidphase method for peptide chain elongation, and then the protectinggroups are all removed with use of an acid. The resulting crude productis purified by, for example, separation and refinement methods, such asgel filtration, ultrafiltration, dialysis, sodium dodecyl sulfatepolyacrylamide gel electrophoresis (SDS-PAGE), and variouschromatographic technologies. It is also possible to selectively acylatethe side chain of the amino acid in a targeted position with use of anacylating enzyme or an acryltransferase.

Also, a production method as a combination of a conventional recombinantDNA technology and a chemical synthesis may be employed. In this case,for example, a fragment having a modified amino acid residue is producedby chemical synthesis, another fragment not having a modified amino acidresidue is separately produced by recombinant DNA technology, and thenthe fragments are fused together to give ghrelin or its derivative (seeaforementioned Patent Literature 1).

Ghrelin and its derivative can be isolated from a natural material.

As used herein, “amino acid” include any and all amino acids, such asL-amino acids, D-amino acids, α-amino acids, β-amino acids, γ-aminoacids, natural amino acids, and synthetic amino acids. Preferred arenatural amino acids.

Adrenomedullin and its Derivative:

Adrenomedullin is a polypeptide having a vasodilatory effect and anantihypertensive effect (blood pressure lowering effect). In vivo, froma precursor of adrenomedullin, a bioactive form of adrenomedullin(activated adrenomedullin) and PAMP (proadrenomedullin N-terminal 20peptide) are biosynthesized (hereinafter, PAMP will be included inadrenomedullin derivatives). Adrenomedullin exerts an effect ofincreasing cAMP in platelets, vascular endothelial cells, and smoothmuscle cells, a platelet aggregation suppressing effect, and a strongvasodilatory and antihypertensive effect.

As used herein, adrenomedullin means activated adrenomedullin unlessotherwise stated.

Regarding human adrenomedullin and its precursor, the amino acidsequence and the cDNA sequence are known.

SEQ ID NO: 11 shows the cDNA base sequence of an adrenomedullinprecursor. SEQ ID NO: 12 shows the amino acid sequence of theadrenomedullin precursor. The amino acid sequence of SEQ ID NO: 12 is anamino acid sequence encoded by the base sequence of SEQ ID NO: 11. SEQID NO: 13 shows the amino acid sequence of adrenomedullin (activatedform). SEQ ID NO: 14 shows the amino acid sequence of PAMP.

As the adrenomedullin, in addition to human adrenomedullin,adrenomedullin of other animals, such as rat, mouse, porcine, bovine,etc. can be used. Preferred is adrenomedullin of a mammal. It ispreferred for each individual to use adrenomedullin of the same species.For example, it is preferred for a human to use human adrenomedullin.

Examples of the adrenomedullin derivative include those having astructure similar to that of adrenomedullin and having effects similarto those of adrenomedullin (an effect of increasing cAMP in platelets ora vasodilatory and/or antihypertensive effect). The adrenomedullinderivative is preferably a polypeptide having an effect of increasingcAMP in platelets, a vasodilatory effect, and an antihypertensiveeffect.

Adrenomedullin derivatives include precursors of adrenomedullin. Also,adrenomedullin derivatives include PAMP.

Specific examples of the adrenomedullin and its derivative of thepresent invention include a polypeptide having a structure selected fromthe following (1) to (3):

(1) a polypeptide having an amino acid sequence represented by SEQ IDNO: 12, 13, or 14,

(2) a polypeptide having an amino acid sequence represented by SEQ IDNO: 12, 13, or 14 in which one to several amino acids are deleted,substituted, and/or added, and

(3) a polypeptide encoded by a nucleic acid capable of hybridizing to anucleic acid consisting of a base sequence represented by SEQ ID NO: 11under stringent condition; and having an effect of increasing cAMP inplatelets or a vasodilatory and/or antihypertensive effect.

In the above (3), the nucleic acid may be any of RNA and DNA, but DNA ispreferred.

The adrenomedullin or its derivative of the present invention ispreferably adrenomedullin (activated form), and more preferablyadrenomedullin of a mammal. The above (1) is preferably a polypeptidehaving an amino acid sequence represented by SEQ ID NO: 13.

In the above (2) of the adrenomedullin or its derivative, the number ofamino acids intended in the “one to several amino acids are deleted,substituted, and/or added” is not particularly limited as long as thepeptide consisting of the amino acid sequence has the desired function.The number is usually about 30 or less (about 1 to 30), preferably about15 or less (about 1 to 15), more preferably about 5 or less (about 1 to5) (for example, preferably about 3 or less (about 1 to 3)), still morepreferably about 1 to 2, and particularly preferably about 1. In casesof substitution or the like with amino acids having similar properties(charge and/or polarity), the desired functions are generally retainedeven if not a few amino acids have been substituted or the like. Incases where substitution or the like occurs at two or more positions,the substitution or the like in all the positions may be deletion only,substitution only, or addition only, or a combination of two or more ofdeletion, substitution, and addition.

Preferably, the amino acid sequence of the adrenomedullin derivativeusually has sequence homology of about 70% or more, preferably about 80%or more, more preferably about 90% or more, particularly preferablyabout 95% or more, and most preferably about 97% or more as comparedwith the amino acid sequence of natural adrenomedullin (for example, SEQID NO: 12, 13, or 14).

As used herein, stringent condition usually means a condition containing6 M urea, 0.4% SDS, and 0.5×SSC, or a hybridization condition havingsimilar stringency. Using a condition of higher stringency, for example,a condition containing 6 M urea, 0.4% SDS, and 0.1×SSC, isolation of aDNA with higher homology can be expected. The DNA isolated in thecondition has high homology or identity at the amino acid level ascompared with the amino acid sequence of the targeted protein.

In the present invention, for example, a nucleic acid capable ofhybridizing to a nucleic acid consisting of the base sequence of SEQ IDNO: 11 under stringent condition is preferably a DNA which usually hassequence homology of about 90% or more, preferably about 95% or more,and more preferably about 98% or more with a DNA consisting of acomplementary base sequence of SEQ ID NO: 11 and which encodes apolypeptide having an effect of increasing cAMP in platelets or avasodilatory and/or antihypertensive effect.

The identity of amino acid sequences or base sequences can usually bedetermined using the algorithm BLAST by Karlin and Altschul. Based onthe algorithm of BLAST, programs called BLASTN or BLASTX have beendeveloped. In cases where analysis of a base sequence is performed usingBLASTN, the parameters are set as score=100 and wordlength=12, forexample. In cases where analysis of an amino acid sequence is performedusing BLASTX, the parameters are set as score=50 and wordlength=3, forexample. Incases where BLAST and Gapped BLAST programs are used, thedefault parameters of each program are used. Detailed procedures ofthese analyzing methods are publicly known.

Whether the adrenomedullin or its derivative has an effect of increasingcAMP in platelets or a vasodilatory and/or antihypertensive effect canbe determined by conducting the tests described in literature byKitamura et al. (Adrenomedullin (11-26): a novel endogenous hypertensivepeptide isolated from bovine adrenal medulla. Kitamura K, Matsui E, KatoJ, Katoh F, Kita T, Tsuji T, Kangawa K, and Eto T. Peptides. 2001November; 22(11): 1713-8.) and literature by Champion et al.(Structure-activity relationships of adrenomedullin in the circulationand adrenal gland. Champion H C, Nussdorfer G G, and Kadowitz P J. RegulPept. 1999 Nov. 30; 85(1): 1-8).

Examples of other forms of the adrenomedullin derivative include anucleic acid which encodes adrenomedullin or an adrenomedullinderivative having a polypeptide structure as described above. Thenucleic acid should be designed to express, when administered in vivo,adrenomedullin or its derivative having the peptide structure asdescribed above.

Adrenomedullin and its derivative can be produced by a conventionalrecombinant DNA technology or a chemical synthesis, or a combinationthereof, etc. Alternatively, it can be isolated from a natural material.

In cases where chemical synthesis is employed, for example, amino acidswith protecting groups are condensed by a liquid phase method and/or asolid phase method for peptide chain elongation, and then the protectinggroups are all removed with use of an acid. The resulting crude productis purified by, for example, separation and refinement methods, such asgel filtration, ultrafiltration, dialysis, sodium dodecyl sulfatepolyacrylamide gel electrophoresis (SDS-PAGE), and variouschromatographic technologies, to give adrenomedullin or its derivative.

Angiotensin II Receptor Antagonist:

An angiotensin II receptor antagonist has an effect of hinderingangiotensin II from binding to an angiotensin II receptor (AT1receptor). The angiotensin II receptor antagonist used as an activeingredient of the present invention may be any agent as long as it hasthe effect.

Examples of the angiotensin II receptor antagonist in the presentinvention include losartan, eprosartan, candesartan, candesartancilexetil, valsartan, telmisartan, irbesartan, tasosartan, olmesartan,olmesartan medoxomil, and azilsartan. Preferred examples of theangiotensin II receptor antagonist in the present invention include oneor more kinds of eprosartan, valsartan, telmisartan, irbesartan,tasosartan, olmesartan, olmesartan medoxomil, and azilsartan, and morepreferred examples include one or more kinds of valsartan, telmisartan,irbesartan, azilsartan, and olmesartan medoxomil. In cases where theangiotensin II receptor antagonist is administered (in combination) withan anticancer and/or antitumor agent, as described later, preferred areone or more kinds of losartan, candesartan cilexetil, valsartan,telmisartan, irbesartan, azilsartan, and olmesartan medoxomil. As theangiotensin II receptor antagonist in the present invention,particularly preferred is telmisartan.

HMG-CoA Reductase Inhibitor:

A HMG-CoA reductase inhibitor has an effect of specifically inhibitingHMG-CoA reductase. The HMG-CoA reductase inhibitor used as an activeingredient of the present invention may be any agent as long as it hasthe effect.

Examples of the HMG-CoA reductase inhibitor in the present inventioninclude natural substances derived from microorganisms, semisyntheticsubstances derived from such natural substances, and completelysynthetic compounds, and specific examples thereof include pravastatin,lovastatin, simvastatin, fluvastatin, rivastatin, atorvastatin,pitavastatin, and rosuvastatin. Among them, preferred are pravastatin,simvastatin, fluvastatin, rivastatin, atorvastatin, pitavastatin, androsuvastatin, and particularly preferred is pitavastatin.

As the above angiotensin II receptor antagonist and the above HMG-CoAreductase inhibitor, commercially available agents or compounds may beused, for example.

The active ingredient in the present invention may be in a free form orin the form of a pharmacologically acceptable salt thereof. Examples ofthe salt include a salt with an inorganic base, a salt with an organicbase, a salt with an inorganic acid, a salt with an organic acid, a saltwith a basic or acidic amino acid, etc.

Preferred examples of the salt with an inorganic base include alkalimetal salts, such as a sodium salt and a potassium salt; alkaline earthmetal salts, such as a calcium salt and a magnesium salt; an aluminumsalt; an ammonium salt; and the like.

Preferred examples of the salt with an organic base include salts withtrimethylamine, triethylamine, pyridine, picoline, ethanolamine,diethanolamine, triethanolamine, dicyclohexylamine,N,N′-dibenzylethylenediamine, and the like.

Preferred examples of the salt with an inorganic acid include salts withhydrochloric acid, hydrobromic acid, nitric acid, sulfuric acid,phosphoric acid, and the like.

Preferred examples of the salt with an organic acid include salts withformic acid, acetic acid, trifluoroacetic acid, fumaric acid, oxalicacid, tartaric acid, maleic acid, citric acid, succinic acid, malicacid, methanesulfonic acid, benzenesulfonic acid, p-toluenesulfonicacid, and the like.

Preferred examples of the salt with a basic amino acid include saltswith arginine, lysine, ornithine, and the like; and preferred examplesof the salt with an acidic amino acid include salts with aspartic acid,glutamic acid, and the like.

The medicinal composition of the present invention is not particularlylimited as long as it comprises the above-mentioned vasoprotective agentor a pharmacologically acceptable salt thereof as an active ingredient.The composition may comprise a publicly known pharmacologicallyacceptable inert carrier, excipient, diluent, etc. In the treatment orprevention method for suppressing or preventing the metastasis of amalignant tumor, it is preferred that a medicinal composition comprisingthe vasoprotective agent is administered to a patient.

Utilizing the medicinal composition, the method for suppressing orpreventing the metastasis of a malignant tumor, and the treatment orprevention method of the present invention, the metastasis of amalignant tumor can be suitably suppressed or prevented. Further, thepresent invention exerts an excellent metastasis suppressing effect evenon a malignant tumor of which the metastasis has been exacerbated oraugmented by an anticancer and/or antitumor agent (for example, aplatinum-based antitumor agent, such as cisplatin). Similarly, thepresent invention exerts an excellent effect even on the metastasis of amalignant tumor of a patient who has undergone resection of a tumor,radiotherapy, or laser ablation treatment. Therefore, according to thepresent invention, it is also possible to suppress or prevent themetastasis of a malignant tumor.

Usually, the metastasis suppressing effect according to the presentinvention is exerted in a manner other than cell-killing or cytostaticaction on a malignant tumor itself. The effect is different from that ofcommon anticancer/antitumor agents which acts on the malignant tumorside, and is an effect of protecting blood vessels or other vessels,that is, an effect exerted on the host (for example, a malignant tumorpatient) side.

Since the effect of the present invention is exerted on the host side,the present invention can exert an excellent metastasis suppressingeffect on any and all kinds of malignant tumors regardless of the kindof the malignant tumor (for example, carcinoma).

The medicinal composition for suppressing or preventing the metastasisof a malignant tumor is suitable also as a medicinal composition forsuppressing or preventing malignant tumor cells from colonizing orinvading vascular endothelium.

The method for suppressing or preventing the metastasis of a malignanttumor, and the treatment or prevention method of the present inventionare suitable also as a method for suppressing or preventing malignanttumor cells from colonizing or invading vascular endothelium.

The medicinal composition, the method for suppressing or preventing themetastasis of a malignant tumor, and the treatment or prevention methodof the present invention can be suitably used for suppressing orpreventing the metastasis of any and all kinds of malignant tumors. Inparticular, they are suitable for suppressing or preventing colonization(adhesion) or invasion of malignant tumor cells to vascular endotheliumduring the process of blood-borne metastasis.

Because of these excellent effects, the present invention is useful notonly for suppression and prevention of the metastasis of a malignanttumor and for prevention etc. of the recurrence after therapeuticresection of a tumor but also for effective suppression or prevention ofthe metastasis of a malignant tumor that is hard to resect.

In addition, angiotensin II receptor antagonists, such as telmisartan;HMG-CoA reductase inhibitors, such as pitavastatin; etc. have alreadybeen clinically administered to a large number of patients, and thesafety has been confirmed. Therefore, the medicinal composition and thetreatment or prevention method of the present invention advantageouslyhave little risk of adverse effects.

An objective of the present invention is to suppress or prevent themetastasis of a malignant tumor, and the intended patients are usuallythose with a malignant tumor. The kind of the malignant tumor is notparticularly limited, and examples thereof include various types, forexample, epithelial malignant tumor, such as carcinoma; non-epithelialmalignant tumor, such as sarcoma; and melanoma.

Examples of the malignant tumor include lung cancer (non-small cell lungcancer, small cell lung cancer, malignant mesothelioma, etc.), gastriccancer, colon cancer, liver cancer, kidney cancer, bladder cancer,pancreatic cancer, thyroid cancer, breast cancer, uterine cancer,ovarian cancer, prostatic cancer, bone tumor, brain tumor, etc.

An objective of the present invention is to suppress or prevent themetastasis of a malignant tumor, and the site of metastasis can be anyand all organs and tissues throughout the body because malignant tumorcells released from a primary tumor (primary lesion) enter the bloodcirculatory system or the lymph system and are diffused to other partsof the body. Malignant tumor cells tend to metastasize to, inparticular, organs and tissues where thin blood vessels such ascapillary are dense and the blood flow is high. In the case of a solidtumor, examples of the most common metastasis site include the lung, thebone, the liver, and the brain. In particular, the lung and the liverare important as sites of metastasis. According to the presentinvention, the metastasis to, for example, tissues or organs, such asthe lung, the bone, the liver, and the brain, more preferably to thelung or the liver can be suppressed or prevented effectively.

The malignant tumor may be a primary tumor or a metastatic tumor, andthe timing of the administration of the medicinal composition of thepresent invention may be anytime after the detection of a malignanttumor, such as carcinoma. In view of the general practice for metastasissuppression, continuous administration or regular administration atcertain intervals is preferred.

The medicinal composition of the present invention is preferablyadministered to a patient who is to undergo or who has undergoneresection of a malignant tumor. A patient who is receiving or who hasreceived administration of an anticancer/antitumor agent is alsopreferable as a subject of administration of the medicinal compositionof the present invention. The anticancer/antitumor agent is, forexample, one or more kinds of anticancer/antitumor agents that are otherthan the medicinal composition of the present invention and can be usedtogether with the medicinal composition of the present invention, andsuch other anticancer/antitumor agents will be described later.

In cases where resection of a malignant tumor, such as carcinoma, isconducted, efficient suppression of the metastasis of the malignanttumor can be achieved as follows. The medicinal composition of thepresent invention is administered to the patient for protection of bloodvessels before the resection, and then the resection is performed. Theblood vessel protection should be continued until the influence ofinflammatory cytokines produced after the resection disappears. Usually,the administration is started about 1 week or more, preferably about 10days or more before the resection, and continued until about 1 week ormore, preferably about 10 days or more after the resection.

The dosage form and the administration route of the medicinalcomposition of the present invention are not particularly limited, andone or more kinds of oral or parenteral agents can be selected dependingon the conditions of the patient. One or more of oral agents and one ormore of parenteral agents can be used in combination.

The medicinal composition of the present invention can be used incombination with at least one of other metastasis-suppressing agents. Assuch a metastasis-suppressing agent, for example, a GC-A agonist, a GC-Bagonist, a NEP inhibitor, a PDE5 inhibitor, a NO donor, an eNOSactivator, a GC-C agonist, a cGMP analog, etc. described in WO2012/118042 can preferably be used.

In cases where one or more of other metastasis-suppressing agents areparenterally, for example intravenously administered, continuousadministration with the use of an infusion pump, a catheter, etc. ispreferably performed. The duration of the continuous administration isseveral hours to several days (for example, about 3 to 14 days,preferably about 3 to 7 days).

In cases where the medicinal composition of the present invention andother metastasis-suppressing agent are used in combination, each can beadministered over the above-mentioned administration durationappropriate for the administration method.

In the present invention, usually, the active ingredient may be mixedwith a publicly known pharmacologically acceptable inert carrier,excipient, diluent, etc. to be formed into a medicinal composition, andadministered to an individual by an administration method conventionallyused in the pharmaceutical field, i.e., oral administration orparenteral administration, such as permucosal administration,intravenous administration, intramuscular administration, andsubcutaneous administration.

For example, in cases where the active ingredient is a peptidesubstance, it may be orally administered as a formulation resistant todegradation in the digestive tract, for example, a microcapsuleformulation based on liposomes encapsulating the peptide as the activeingredient. The administration can be performed not through the mucosaof the digestive tract but through, for example, the rectal, intranasal,or sublingual mucosa. In this case, the active ingredient can beadministered to an individual in the form of, for example, asuppository, a nasal spray, an inhalant, a sublingual tablet, etc. Inthe present invention, such formulations may be used that the peptideretention in the blood is improved by adopting variouscontrolled-release formulations or long-acting formulations whichcomprise a biodegradable polymer represented by polysaccharide such asdextran, polyamine, PEG, etc. as a carrier.

When the active ingredient is in the form of a nucleic acid encoding apeptide substance, the nucleic acid (such as a gene encoding a peptidesubstance) may be introduced into a patient via intravenous injection,intramuscular injection, local injection, or the like using a viralvector such as a retrovirus, an adenovirus, and an adeno-associatedvirus, or using a plasmid vector etc.

The dosage amount of the substance used as an active ingredient of themedicinal composition of the present invention varies with the type ofdisease (malignant tumor); the age, body weight, and degree of thesymptoms of the individual (patient); and the route of administration,and can be selected as appropriate, but generally the upper limit of thedaily dosage of each active ingredient is, for example, usually about100 mg/kg or less, preferably about 50 mg/kg or less, and morepreferably about 1 mg/kg or less. The lower limit of the daily dosage ofeach active ingredient is, for example, usually about 0.1 μg/kg or more,preferably about 0.5 μg/kg or more, and more preferably about 1 μg/kg ormore. The dosage amount is expressed as an amount per kilogram of bodyweight.

In cases where the active ingredient is ghrelin or its derivative, theadministration rate is, for example, continuous administration of about0.1 μg/kg/min or less, preferably about 0.08 μg/kg/min or less, or thelike.

In cases where the active ingredient is adrenomedullin or itsderivative, the administration rate is usually continuous administrationof about 0.1 μg/kg/min or less, preferably about 0.05 μg/kg/min or less,or the like.

The duration of the continuous administration of ghrelin,adrenomedullin, or a derivative thereof is usually about one day orlonger, and preferably about 1 day to about 2 weeks. In the continuousadministration, a preferred administration method is intravenousadministration, or the like.

The administration frequency of the active ingredient in the medicinalcomposition, the treatment or prevention method, or the like of thepresent invention is not particularly limited and varies with the activeingredient to be used, the route of administration, and the specificdisease to be treated.

In cases where ghrelin, adrenomedullin, or a derivative thereof isorally administered, a preferable frequency of the administration is forexample about 4 times or less daily. In cases of parenteraladministration, for example intravenous administration, continuousadministration with the use of an infusion pump, a catheter, etc. ispreferred.

In cases where an angiotensin II receptor antagonist or a HMG-CoAreductase inhibitor is orally administered, the agent is preferablyadministered, for example, about once to 3 times daily. For example, incases where an angiotensin II receptor antagonist or a HMG-CoA reductaseinhibitor is used, the agent is preferably orally administered in adaily amount of about 1 to 100 mg/kg body weight of the activeingredient, and the dosage amount is comparable to or less than thatused for hypertension or hypercholesterolemia.

The medicinal composition, the treatment or prevention method, or thelike of the present invention, when combined with at least one of otherusually used anticancer and/or antitumor agents, can achieve moreeffective treatment of a malignant tumor. The present inventionencompasses such a combination treatment with another anticancer and/orantitumor agent. An example of such a combination treatment is anembodiment in which the medicinal composition of the present inventionis administered to a patient who is receiving or who has receivedadministration of an anticancer/antitumor agent. Since the medicinalcomposition of the present invention can control the metastasis andinvasion of tumor cells, appropriate administration of the medicinalcomposition during a treatment using another anticancer and/or antitumoragent can increase the efficiency of the treatment with the anticancerand/or antitumor agent and can improve the prognosis of the treatment.

By using the vasoprotective agent or a pharmacologically acceptable saltthereof with at least one of other usually used anticancer and/orantitumor agents, an effect of effectively suppressing or preventingexacerbation and/or augmentation of metastasis of a malignant tumorcaused by the anticancer and/or antitumor agent can also be obtained.

The medicinal composition of the present invention is preferably usedfor suppressing or preventing exacerbation and/or augmentation ofmetastasis of a malignant tumor caused by an anticancer and/or antitumoragent.

The present invention encompasses a method for suppressing or preventingexacerbation and/or augmentation of metastasis of a malignant tumorcaused by an anticancer and/or antitumor agent, the method comprisingadministering an effective amount of a vasoprotective agent or apharmacologically acceptable salt thereof to a patient.

In cases where the medicinal composition of the present invention isadministered (in combination) with an anticancer and/or antitumor agent,the dosage amount of the anticancer and/or antitumor agent is notparticularly limited and can be set as appropriate depending on the typeof the agent, the type of disease (malignant tumor); the age, bodyweight, and degree of the symptoms of the individual (patient); and theroute of administration, and is a usually used amount.

In cases where the medicinal composition of the present invention isadministered (in combination) with an anticancer and/or antitumor agent,the dosage amount of the medicinal composition of the present inventionvaries with the type of disease (malignant tumor); the age, body weight,and degree of the symptoms of the individual (patient); and the route ofadministration, and is appropriately selected. Regarding the dosageamount of the vasoprotective agent or a pharmacologically acceptablesalt thereof as an active ingredient, in cases where an angiotensin IIreceptor antagonist or a HMG-CoA reductase inhibitor is used forexample, preferably about 1 to 100 mg/kg body weight of the activeingredient is orally administered daily, and the dosage amount iscomparable to or less than that used for hypertension orhypercholesterolemia.

Incases where an anticancer/antitumor agent (for example, aplatinum-based antitumor agent, such as cisplatin) is administered,efficient suppression of the metastasis (distant metastasis andrecurrence) of a malignant tumor can be achieved as follows. Themedicinal composition of the present invention is administered to thepatient for preliminary protection of blood vessels, and then theanticancer/antitumor agent is administered. The blood vessel protectionshould be continued until the anticancer/antitumor agent is eliminatedfrom the body. Usually, the administration of the medicinal compositionof the present invention is started about 1 week or more, preferablyabout 10 days or more before the start of the administration of theanticancer/antitumor agent, and continued until about 1 week or more,preferably about 10 days or more after the end of the administration ofthe anticancer/antitumor agent.

Incases where an anticancer/antitumor agent (for example, aplatinum-based antitumor agent, such as cisplatin) is administered, oneor more kinds of oral or parenteral agents can be selected as themedicinal composition for the present invention depending on theconditions of the patient. One or more of oral agents and one or more ofparenteral agents can be used in combination.

The medicinal composition of the present invention can be used incombination with at least one of said other metastasis-suppressingagents.

Incases where an anticancer/antitumor agent (for example, aplatinum-based antitumor agent, such as cisplatin) is administered, themedicinal composition of the present invention and othermetastasis-suppressing agents used in combination can be administered atthe same time or at different times.

In such a combined administration, the administration of the medicinalcomposition of the present invention is usually started about 1 week ormore, preferably about 10 days or more before the start of theadministration of the anticancer/antitumor agent, and continued untilabout 1 week or more, preferably about 10 days or more after the end ofthe administration of the anticancer/antitumor agent.

The dosage form and the administration route of the medicinalcomposition of the present invention are not particularly limited, andone or more kinds of oral or parenteral agents can be selected dependingon the conditions of the patient. One or more of oral agents and one ormore of parenteral agents can be used in combination.

In such a combined administration, in cases where one or more of othermetastasis-suppressing agents are parenterally, for exampleintravenously administered, continuous administration with the use of aninfusion pump, a catheter, etc. is preferably performed. The duration ofthe continuous administration is about several hours to several days(for example, about 3 to 14 days, preferably about 3 to 7 days).

In cases where the medicinal composition of the present invention andanother metastasis-suppressing agent are used in combination, each canbe administered over the above-mentioned administration durationappropriate for the administration method.

In cases where the medicinal composition of the present invention oranother metastasis-suppressing agent is administered, the administrationis preferably performed depending on the condition of the patient asfollows. For example, before resection or administration of ananticancer/antitumor agent, the medicinal composition of the presentinvention (for example, an angiotensin II receptor antagonist or aHMG-CoA reductase inhibitor) or said another metastasis-suppressingagent is orally administered. After the resection or the administrationof the anticancer/antitumor agent, i.e., during a period in which oraladministration of medicinal agents etc. cannot be performed, a medicinalcomposition of the present invention (for example, ghrelin or itsderivative, or adrenomedullin or its derivative) or said anothermetastasis-suppressing agent is parenterally administered, and afterrecovery, the medicinal composition of the present invention or anothermetastasis-suppressing agent is orally administered.

Examples of the anticancer/antitumor agent used in combination with themedicinal composition of the present invention include an alkylatingagent, an antimetabolite, an antitumor antibiotic, an antitumor plantconstituent, a BRM (biological response control substance), a hormone, avitamin, an anticancer antibody, a molecular target agent, aplatinum-based antitumor agent, other anticancer/antitumor agents, etc.Among them, preferred as an anticancer/antitumor agent used incombination with the medicinal composition of the present invention is aplatinum-based antitumor agent.

More specifically, examples of the alkylating agent include alkylatingagents, such as nitrogen mustard, nitrogen mustard N-oxide andchlorambucil; aziridine alkylating agents, such as carboquone andthiotepa; epoxide alkylating agents, such as dibromomannitol anddibromodulcitol; nitrosourea alkylating agents, such as carmustine,lomustine, semustine, nimustine hydrochloride, streptozocin,chlorozotocin, and ranimustine; busulfan; improsulfan tosilate;dacarbazine; etc.

Examples of various antimetabolites include purine antimetabolites, suchas 6-mercaptopurine, 6-thioguanine, and thioinosine; pyrimidineantimetabolites, such as fluorouracil, tegafur, tegafur-uracil,carmofur, doxifluridine, broxuridine, cytarabine, and enocitabine;folate antimetabolites, such as methotrexate and trimetrexate; etc.

Examples of the antitumor antibiotic include anthracycline antibioticantitumor agents, such as mitomycin-C, bleomycin, peplomycin,daunorubicin, aclarubicin, doxorubicin, pirarubicin, THP-adriamycin,4′-epidoxorubicin, and epirubicin; chromomycin A3; actinomycin-D; etc.

Examples of the antitumor plant constituent include vinca alkaloids,such as vindesine, vincristine, and vinblastine; taxanes, such aspaclitaxel and docetaxel; epipodophyllotoxins, such as etoposide andteniposide.

Examples of the BRM include a tumor necrosis factor, indomethacin, etc.

Examples of the hormone include hydrocortisone, dexamethasone,methylprednisolone, prednisolone, prasterone, betamethasone,triamcinolone, oxymetholone, nandrolone, methenolone, fosfestrol,ethinylestradiol, chlormadinone, medroxyprogesterone, etc.

Examples of the vitamin include vitamin C, vitamin A, etc.

Examples of the antitumor antibody and the molecular target agentinclude trastuzumab, rituximab, cetuximab, nimotuzumab, denosumab,bevacizumab, infliximab, imatinib mesylate, gefitinib, erlotinib,sunitinib, lapatinib, sorafenib, etc.

Examples of the platinum-based antitumor agent include cisplatin,carboplatin, oxaliplatin, etc. Among them, cisplatin is preferred.

Examples of other anticancer/antitumor agents include tamoxifen,camptothecin, ifosfamide, cyclophosphamide, melphalan, L-asparaginase,aceglatone, sizofiran, picibanil, procarbazine, pipobroman,neocarzinostatin, hydroxyurea, ubenimex, krestin, etc.

In the present invention, when additional anticancer/antitumor agents(or metastasis-suppressing agents) are administered in combination withthe vasoprotective agent, one or more kinds of the vasoprotective agentsand the additional anticancer/antitumor agents (ormetastasis-suppressing agents) may be contained as active ingredients ina single formulation or in separate formulations.

In cases where the medicinal composition of the present invention isused with an anticancer and/or antitumor agent, the combination of thevasoprotective agent or a pharmacologically acceptable salt thereof andthe anticancer and/or antitumor agent is not particularly limited, butfor example, when the anticancer or antitumor agent is a platinum-basedantitumor agent, such as cisplatin, the vasoprotective agent ispreferably an angiotensin II receptor antagonist or a HMG-CoA reductaseinhibitor. Angiotensin II receptor antagonists and HMG-CoA reductaseinhibitors can effectively suppress exacerbation and/or augmentation ofmetastasis of a malignant tumor caused by a platinum-based antitumoragent. The angiotensin II receptor antagonist is preferably one or morekinds of telmisartan, valsartan, losartan, olmesartan medoxomil,azilsartan, candesartan cilexetil, and irbesartan. The HMG-CoA reductaseinhibitor is preferably pitavastatin. The platinum-based antitumor agentto be used in combination with the angiotensin II receptor antagonist orthe HMG-CoA reductase inhibitor is preferably cisplatin.

In the present invention, “combined administration” of multiple activeingredients or drugs means that a subject to receive the administrationtakes all the combined active ingredients or drugs into the body in acertain period of time. The active ingredients may be administered as asingle formulation containing all the ingredients (so-called compoundingagent). Alternatively, the active ingredients may be separatelyformulated into separate formulations and then separately administered(so-called administration based on combined use). In cases where theactive ingredients are separately formulated, the timing of theadministration is not particularly limited. The formulations may beadministered simultaneously, on the same day at certain time intervals,or on different days. In cases where two or more active ingredients areadministered at different timings of the same day or on different days,the order of administration of the active ingredients is notparticularly limited. Normally, each formulation is administeredaccording to each administration method, and therefore the frequency ofthe administration may be the same or different among the formulations.In cases where each active ingredient is separately formulated, theadministration method (route of administration) may be the same ordifferent among the formulations. It is not necessary that all theactive ingredients are present in the body at the same time. As long asall the active ingredients are taken into the body during a certainperiod of time (for example, one month, preferably one week, morepreferably several days, still more preferably one day), it is allowablethat one active ingredient has already disappeared from the body whenanother active ingredient is administered.

EXAMPLES

Hereinafter, the invention will be specifically described by referringto the Examples below. The Examples are merely illustrative examples ofthe embodiments of the present invention, and the present invention isnot limited thereto.

The experimental materials used in the Examples below were obtained andprepared as follows.

The cisplatin (CDDP) used was CISPLATIN inj. “Maruko” (Nichi-IkoPharmaceutical). The osmotic pumps used were MODEL2002 (for 14-dayadministration) made by ALZET (Cupertino, Calif.). Ghrelin (a peptideconsisting of the amino acid sequence of SEQ ID NO: 1 in which the sidechain hydroxyl group of the serine residue at the 3rd position from theamino terminus is octanoylated) andadrenomedullin (SEQIDNO: 13) wereobtained, each in the form of a lyophilized product, from Asubio PharmaCo., Ltd., and the lyophilized products were separately dissolved inphysiological saline. After the concentrations were adjusted asappropriate, the solutions were used in the following experiments. Thechi-squared test was used to determine whether there was a significantdifference (*: P<0.05) in the Examples.

Example 1 Lung Metastasis Suppressing Effects of Various BioactivePeptides and Agents in Blood-Borne Metastasis Model Established byInjection of Mouse Melanoma to Mouse Tail Vein

Six-week-old male C56BL/6N mice (purchased from Japan SLC, Inc.) wereused. Mouse melanoma B16-F10 was purchased from ATCC, and cultured inDMEM (Life Technologies Corp.) containing 10% FCS under 5% CO₂ at 37° C.The cells in a subconfluent state were treated with EDTA-trypsin,centrifuged, and then suspended in serum free DMEM so as to be 5×10⁶cells/mL. The melanoma cell suspension (100 μL/mouse, 5×10⁵ cells) wasinjected to the tail vein of the mice.

For the CDDP group, 5 mg/kg of CDDP was injected, as pretreatment, tothe tail vein of the mice 2 days before the injection of the melanomacells into the tail vein. For the control group, an osmotic pumpcontaining 0.9% physiological saline was subcutaneously implanted in theback of each mouse on the day before the injection of the melanoma cellsinto the tail vein. Similarly, for the adrenomedullin group, an osmoticpump containing adrenomedullin prepared for administration at 0.05μg/kg/min was subcutaneously implanted into each mouse, and for theghrelin group, an osmotic pump containing ghrelin prepared foradministration at 0.08 μg/kg/min was subcutaneously implanted into eachmouse. The tail vein injection of the melanoma cells was performed asabove and the drug administration was continued for 2 weeks. Thecondition of the lung metastasis of the tumor cells 2 weeks after thetumor cell injection was observed (FIG. 1). FIG. 2 shows the number ofobserved nodules per animal formed due to lung metastasis.

To the angiotensin II receptor antagonist group, a 0.5% methylcelluloseaqueous solution prepared so as to contain 2 mg/kg or 8 mg/kg oftelmisartan was orally given for 4 days before the start of theexperiment (before the injection of tumor cells to mice), and to thepitavastatin group, a 0.5% methylcellulose aqueous solution prepared soas to contain 20 mg/kg of pitavastatin was orally given for the sameperiod. After the injection of tumor cells, the oral intake ofmethylcellulose aqueous solutions containing telmisartan or pitavastatinin the above doses in the angiotensin II receptor antagonist group andthe pitavastatin group was continued until the end of the experiment. Tothe control group, a 0.5% methylcellulose aqueous solution notcontaining any of the agents was orally given before the start of theexperiment. Also, as reference example, angiotensin II was administeredat 1 μg/kg/min, and then the experiment was conducted in the same way.The sample size of each group was n=5.

As a result, as shown in FIGS. 3 and 4, the lung metastasis of melanomawas significantly suppressed in the telmisartan 8 mg/kg group. Also, asshown in FIG. 4, the lung metastasis of melanoma was significantlyincreased in the CDDP group as compared to the control group. Incontrast, in both of the telmisartan 2 mg/kg group and the telmisartan 8mg/kg group, the exacerbation by CDDP was suppressed. The telmisartan 2mg/kg (CDDP group) and the telmisartan 8 mg/kg (CDDP group) shown inFIGS. 3 and 4 are groups to which 2 mg/kg or 8 mg/kg of telmisartan wasgiven in the manner described above before CDDP was injected aspretreatment. The pitavastatin (CDDP group) is the group to whichpitavastatin was given in the manner described above before CDDP wasinjected as pretreatment.

Meanwhile, as shown in FIGS. 5 and 6, the exacerbation of the lungmetastasis by CDDP was significantly suppressed in the pitavastatingroup.

Example 2 Lung Metastasis Suppressing Effects of Various Agents inBlood-Borne Metastasis Model Established by Injection of Mouse Melanomato Mouse Tail Vein

Eight-week-old male C57BL6 mice (purchased from Japan SLC, Inc.) wereused. Mouse melanoma B16-F10 was purchased from ATCC, and cultured inDMEM (Life Technologies Corp.) containing 10%

FCS under 5% CO₂ at 37° C. The cells in a subconfluent state weretreated with EDTA-trypsin, centrifuged, and then suspended in serum freeDMEM so as to be 5×10⁶ cells/mL. The melanoma cell suspension (100μL/mouse, 3×10⁵ cells) was injected to the tail vein of the mice.

As pretreatment, 5 mg/kg of cisplatin (CDDP) was injected to the tailvein of the mice 2 days before the injection of the melanoma cells intothe tail vein.

As an angiotensin II receptor antagonist, used were valsartan (tradename: Diovan made by Novartis Pharma K.K.), losartan (trade name:Nu-Lotan made by MSD K.K.), olmesartan medoxomil (trade name:Olmetecmade by Daiichi Sankyo Co., Ltd.), azilsartan (trade name: Azilvamade by Takeda Pharmaceutical Co., Ltd.), candesartan cilexetil (tradename: Blopress made by Takeda Pharmaceutical Co., Ltd.), and irbesartan(trade name: Avapro made by Sumitomo Dainippon Pharma Co., Ltd.).

To the angiotensin II receptor antagonist group, a 0.5% methylcelluloseaqueous solution prepared so as to contain valsartan (40 mg/kg),losartan (30 mg/kg), olmesartan medoxomil (5 mg/kg), azilsartan (10mg/kg), candesartan cilexetil (8 mg/kg), or irbesartan (100 mg/kg) wasorally given for 4 days before the start of the experiment (before theinjection of tumor cells to mice). After the injection of tumor cells,the oral intake of methylcellulose aqueous solutions containingtelmisartan or pitavastatin in the above doses in the angiotensin IIreceptor antagonist group and the pitavastatin group was continued untilthe end of the experiment. To the control group, a 0.5% methylcelluloseaqueous solution not containing any of the agents was orally givenbefore the start of the experiment. The sample size of each group wasn=5.

The condition of the lung metastasis of the tumor cells 2 weeks (14days) after the tumor cell injection was observed. The results are shownin FIG. 7. FIG. 8 shows the number of observed nodules per animal formeddue to lung metastasis (average and standard deviation of n=5).

FIGS. 7 and 8 show that the administration of cisplatin (CDDP) augmentedtumor metastasis, but valsartan, losartan, olmesartan medoxomil,azilsartan, candesartan cilexetil, and irbesartan significantlysuppressed the exacerbation of lung metastasis caused by CDDP.

Example 3 Vasoprotective Effect on Human Lung Arterial MicrovascularEndothelial Cells

Human lung arterial microvascular endothelial cells (manufactured byLonza Japan) were cultured to confluence, losartan was added thereto (toa final concentration of 5×10⁻⁶ M), and 2 hours later, phosphatebuffered saline (PBS) or cisplatin (CDDP) was added (to a finalconcentration of 5 μM). An hour later, the culture medium was replacedwith a fresh culture medium (Medium 199 (of Gibco brand manufactured byInvitrogen) containing 1% bovine serum albumin (BSA) manufactured bySigma). To this, a suspension of fluorescently-labeled A549-GFP humanlung cancer cells (manufactured by AntiCancer Japan) (1×10⁵ cells) wasadded, and the endothelial cells and lung cancer cells were co-culturedfor 3 hours. As a result, the 1-hour pretreatment with 5 μM CDDPincreased the number of cancer cells adhered to the vascular endothelialcells, but the pretreatment with losartan (5×10⁻⁶M) performed 2 hoursbefore the CDDP pretreatment significantly suppressed the adhesion ofcancer cells to the vascular endothelial cells. The results are shown inFIGS. 9A and 9B.

INDUSTRIAL APPLICABILITY

The present invention provides an excellent medicinal compositioncapable of suppressing the metastasis of a malignant tumor, a method forsuppressing or preventing the metastasis, and a method for treating orpreventing the metastasis of a malignant tumor. Further, the presentinvention exerts an excellent metastasis suppressing effect even on amalignant tumor of which the metastasis has been exacerbated by ananticancer and/or antitumor agent. Therefore, the present invention isuseful in the fields of medicine etc.

1. A method for suppressing or preventing the metastasis of a malignanttumor, the method comprising administering, to a patient, an effectiveamount of at least one kind of vasoprotective agent selected from thegroup consisting of: (i) adrenomedullin or its derivative, (ii) ghrelinor its derivative, (iii) HMG-CoA reductase inhibitor, and or apharmacologically acceptable salt thereof.
 2. A method for suppressingor preventing exacerbation and/or augmentation of metastasis of amalignant tumor caused by an anticancer and/or antitumor agent, themethod comprising administering, to a patient, an effective amount of atleast one kind of vasoprotective agent selected from the groupconsisting of: (i) adrenomedullin or its derivative, (ii) ghrelin or itsderivative, (iii) HMG-CoA reductase inhibitor, and (iv) angiotensin IIreceptor antagonist; or a pharmacologically acceptable salt thereof.3-17. (canceled)
 18. The method of claim 1, wherein the adrenomedullinor its derivative is a polypeptide having a structure selected from thegroup consisting of: (1) a polypeptide having an amino acid sequencerepresented by SEQ ID NO: 12, 13, or 14, (2) a polypeptide having anamino acid sequence represented by SEQ ID NO: 12, 13, or 14 in which oneto several amino acids are deleted, substituted, and/or added, and (3) apolypeptide encoded by a nucleic acid capable of hybridizing to anucleic acid consisting of a base sequence represented by SEQ ID NO: 11under stringent condition; and having an effect of increasing cAMP inplatelets or a vasodilatory and/or antihypertensive effect.
 19. Themethod of claim 1, wherein the ghrelin or its derivative is a peptidehaving a structure selected from the group consisting of: (1) a peptidehaving an amino acid sequence represented by any one of SEQ ID NOs:1 to10 in which the amino acid residue at the 3rd position from the aminoterminus is a modified amino acid residue having a side chain acylatedwith a fatty acid, (2) a peptide having an amino acid sequencerepresented by any one of SEQ ID NOs: 1 to 10 in which one to severalamino acids are deleted, substituted, and/or added and the amino acidresidue at the 3rd position from the amino terminus is a modified aminoacid residue having a side chain acylated with a fatty acid, and (3) apeptide having an amino acid sequence represented by any one of SEQ IDNOs: 1 to 10 in which the sequence from the amino terminus to at leastthe 4th position is conserved, one to several amino acids are deleted,substituted, and/or added not in the conserved sequence, and the aminoacid residue at the 3rd position from the amino terminus is a modifiedamino acid residue having a side chain acylated with a fatty acid; andhaving an agonistic effect on growth hormone secretagogue receptor 1 a.20. The method of claim 1, wherein the HMG-CoA reductase inhibitor isselected from the group consisting of pravastatin, lovastatin,simvastatin, fluvastatin, rivastatin, atorvastatin, pitavastatin, androsuvastatin.
 21. The method of claim 20, wherein the HMG-CoA reductaseinhibitor is pitavastatin.
 22. The method of claim 1, wherein theangiotensin II receptor antagonist is selected from the group consistingof losartan, eprosartan, candesartan, candesartan cilexetil, valsartan,telmisartan, irbesartan, tasosartan, olmesartan, olmesartan medoxomil,and azilsartan.
 23. The method of claim 22, wherein the angiotensin IIreceptor antagonist is selected from the group consisting of valsartan,telmisartan, irbesartan, olmesartan medoxomil, and azilsartan.
 24. Themethod of claim 22, wherein the angiotensin II receptor antagonist istelmisartan.
 25. The method of claim 1, wherein the metastasis of themalignant tumor is metastasis to the lung, the bone, the liver, or thebrain.
 26. The method of claim 25, wherein the metastasis of themalignant tumor is metastasis to the lung or the liver.
 27. The methodof claim 1, wherein the malignant tumor is selected from the groupconsisting of epithelial malignant tumor, non-epithelial malignanttumor, and melanoma.
 28. The method of claim 27, wherein the malignanttumor is melanoma.
 29. The method of claim 1, wherein a subject ofadministration is a patient who is to undergo or who has undergoneresection of a malignant tumor.
 30. The method of claim 1, wherein asubject of administration is a patient who is receiving or who hasreceived administration of an anticancer/antitumor agent.
 31. The methodof claim 1, which is for use in combination with an anticancer/antitumoragent.
 32. The method of claim 31, wherein the anticancer/antitumoragent is a platinum-based antitumor agent.